QC Supervisor
Core
Provide leadership within Quality Control ensuring compliance with cGMP standards and regulatory requirements for pharmaceutical manufacturing from raw materials to finished products.
Role type
QC Supervisor
Builds
Pharmaceutical products and quality documentation
Domain
Pharmaceutical manufacturing / Quality Control
Required skills
cGMP compliance, FDA regulations, ICH guidelines, analytical testing methods, HPLC, GC, dissolution testing, team leadership, technical writing, LIMS, quality management software, project management, risk assessment, root cause analysis
Preferred skills
Chemistry, Biology, Biochemistry, Microbiology, quality systems certification, regulatory compliance certification, project management certification
Technologies
HPLC, GC, dissolution testing equipment, LIMS, quality management software, Microsoft Office
Responsibilities
Provide technical leadership and oversight for laboratory operations, mentor staff, optimize workflows, implement continuous improvement initiatives, support regulatory audits and inspections, manage laboratory operations including scheduling and resource planning
Seniority
Mid-level, hands-on IC with leadership responsibilities
